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FDA Acquiring ‘Fresh’ Aborted Baby Parts to Make Mice With Human Immune Systems
By Terence P. Jeffrey | August 7, 2018 | 11:48 AM EDT



(NIH Video/Screen Capture)
(CNSNews.com) - The U.S. Food and Drug Administration signed a new contract on July 25 to acquire “fresh” human fetal tissue to transplant into “humanized mice” so that these mice will have a functioning “human immune system,” according to information published by the FDA and the General Services Administration.
“The objective is to acquire Tissue for Humanized Mice,” said a June 13 FDA “presolicitation notice” for the contract.
The contractor, the notice said, would “provide the human fetal tissue needed to continue the ongoing research being led by FDA.
“Fresh human tissues are required,” said the notice, “for implantation into severely immune-compromised mice to create chimeric animals that have a human immune system.”
According to GSA’s federal contract database, Advanced Bioscience Resources (ABR), a non-profit organization based in the San Francisco Bay Area, was awarded this $15,900 contract, which will run through July 25, 2019.
“Fetal tissue used in research is obtained from elective abortions,” says the Congressional Research Service.
In 2016, Harvard University provided the House Energy and Commerce Committee’s Select Investigative Panel on Infant Lives with a background paper explaining that mice with human immune systems “are engineered to this condition only by means of the use of human fetal material” and that this material can only come from aborted babies not from miscarriages. (See the Harvard backgrounder by clicking here.)
Thus, by issuing a contract to acquire human fetal tissue to use in making mice with human immune systems, the FDA is using federal tax dollars to create a demand for human body parts that must be taken from babies who are aborted.
Because it would not be able to create its “humanized mice” without fresh tissue taken from aborted babies, the FDA also has an interest in the continuation of legalized abortions at a stage in fetal development when the tissue needed to create these mice can be retrieved from the aborted baby.

The above graphic depicting the creation of a humanized mouse was included in a November 2016 FDA presentation posted on the FDA's website.
While the FDA confirmed to CNSNews.com that its June 13 presolicitation notice for a contract to “acquire Tissue for Humanized Mice” and the July 25 contract it signed with ABR (as reported on the GSA contract database) refer to the same deal, the FDA declined to answer 17 other questions CNSNews.com asked it about that contract and the aborted baby parts it requires the contractor to provide. (See the full set of questions CNSNews.com sent to the FDA by clicking here.)
Instead the FDA provided CNSNews.com with a three-paragraph statement. (See the FDA’s full statement by clicking here.)
In its specific questions, CNSNews.com asked the FDA to disclose:
--The total number of babies expected to donate their tissue to the FDA to create humanized mice during the year-long duration of the contract.
--Whether the FDA needed to know that the abortion of a donor baby was taking place so FDA researchers could be prepared to implant this baby’s “fresh” tissue into mice in a timely manner.
--What the minimum and maximum gestational ages of the babies must be to provide the tissue needed to create these “humanized mice.”
--Whether there were any methods of abortion that could not be used to terminate the babies whose tissue would be used by the FDA to create humanized mice because that method would cause the tissue to be damaged or spoiled in a way that would make it unsuitable for this research.
The FDA also would not answer this question: “Are the mothers who agree to donate the tissue from their unborn babies for this FDA research informed that tissue taken from their aborted baby will be transplanted into a mouse?”
In its statement to CNSNews.com, the FDA stressed that it was committed to making certain its research followed “all legal requirements” and met “the highest ethical standards.”
“The U.S. Food and Drug Administration is committed to ensuring that its research is conducted responsibly, conforms with all legal requirements, and meets the highest ethical standards,” said the FDA statement.
“At the FDA, research involving human fetal tissue accounts for a very small fraction of the FDA’s total research and has been used in situations where it is critical to understanding how the human immune system responds to certain drugs and biologics,” the statement said. “This work has led to a better understanding of a number of conditions and diseases that affect millions of Americans.
“The FDA’s researchers obtain fetal tissue from a non-profit Tissue Procurement Organization (TPO) that have [sic] provided assurances that they are in compliance with all applicable legal requirements, including relevant provisions relating to research involving human fetal tissue,” said the statement.
“FDA is not involved in the TPO’s sourcing of the tissue,” it said.
“In addition,” the statement continued, “the FDA has in place systems to ensure FDA research using fetal tissue, as well as any research funded by FDA, is in compliance with applicable federal, state and local regulations and guidelines, as well as FDA policies.”
Since 2012, according to the GSA’s Federal Procurement Data System, the FDA has signed eight contracts with ABR, including the one signed July 25. Seven of these expressly cite “Humanized Mice,” “Human Fetal Tissue” or “Tissue Procurement for Humanized Mice” in the contract’s “description of requirement.” The eighth simply says: “Human Tissue.”
The “description of requirement” for the latest contract is only two words long. It says: “Humanized Mice.”
The FDA’s most recent prior contract with ABR ran from July 13, 2017 to July 12, 2018. It carried this description: “Tissue Procurement for Humanized Mice—other functions.”
Before that, the FDA had a contract with ABR that ran from May 10, 2016 to May 15, 2017. Its description of requirement said: “Human Fetal Tissue (Liver/Thymus).”

This screen capture from the GSA database listing of the contract that the FDA signed with ABR on May 10, 2016 has as the description of requirement "Human Fetal Tissue (Liver/Thymus)"
The FDA’s June 13 presolicitation notice contended that Advanced Biosciences Resources was the only organization that could fulfill the new contract.
“ABR is the only company in the U.S. capable of supplying tissue suitable for HM research. No other company or organization is capable of fulfilling the need,” the FDA notice said.
“The government intends to solicit and negotiate directly with Advanced Bioscience Resources (ABR) Inc., and no solicitation will be issued,” it said.
“The objective is to acquire Tissue for Humanized Mice,” it said.

more at  https://www.cnsnews.com/news/article/terence-p-jeffrey/fda-acquiring-fresh-aborted-baby-parts-make-mice-human-immune-systems
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